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17

抑制剂 & 化合物

5

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T6532	Hesperadin	Influenza Virus; Parasite; Aurora Kinase; Autophagy	Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Microbiology/Virology
	Hesperadin 是 Aurora A 和 B 的 ATP 竞争性吲哚酮抑制剂，抑制 Aurora B 的 IC50值为250nM。它通过阻断核分裂和胞质分裂而抑制布鲁氏锥虫的生长。它也是一种广谱流感抗病毒剂。
T4179	Probucol disuccinate	LDL	Metabolism
	Probucol disucinate 是一种 Probucol 的衍生物。其中 Probucol 是脂质调节的化合物，它能降低 LDL-cholesterol 水平。
T4582	xanthanol NSC 4038,占吨氢醇	Others	Others
	Xanthanol(NSC 4038) 用于测试血液中的尿素水平。
TP2107L	Histrelin acetate Histrelin acetate(76712-82-8 free base),醋酸组氨瑞林	GNRH Receptor	GPCR/G Protein
	Histrelin acetate 是促性腺激素释放激素 (GnRH) 的九肽类似物，具有增加的效力。当存在于血流中时，它作用于称为促性腺激素的垂体特定细胞。 Histrelin 刺激这些细胞释放促黄体激素和促卵泡激素。因此，它被认为是促性腺激素释放激素激动剂或 GnRH 激动剂。
T70673	NEU617
	NEU617 is an inhibitor of the growth of protozoan parasites, against T. brucei bloodstream proliferation.
T25490	Hemorphin 4 Tyr-pro-trp-thr
	Hemorphin 4 is an endogenous opioid peptide of the hemorphin family which has antinociceptive properties and is derived from the β-chain of hemoglobin in the bloodstream.
T38967	DSPE-PEG(2000)
	MPEG-2000-DSPE sodium is a phospholipid PEG conjugate with hydrophilicity and hydrophobicity. It is utilized in liposome synthesis to enhance the hydrophilicity of liposomes, thereby prolonging their circulation in the bloodstream. This compound is commonly employed for the investigation of anticancer and antimalarial agents.
T31215	DB-766 DB766
	DB-766 is a potential chemotherapeutic candidate for Chagas' disease treatment. DB-766 exhibits strong trypanocidal activity and excellent selectivity for bloodstream trypomastigotes and intracellular amastigotes (Y strain), giving IC(50)s of 60 and 25 nM
T79457	PEX5-PEX14 PPI-IN-1
	PEX5-PEX14 PPI-IN-1(Compound 8)为PEX14-PEX5 PPI 抑制剂，其通过破坏PEX5-TbPEX14 PPI的作用并表现出53 μM的Ki值。该化合物还能抑制T. b. brucei的bloodstream形式，EC50为5 μM。
T14967	Cimlanod BMS-986231,CXL-1427	Others	Others
	Cimlanod is a second-generation Nitroxyl (HNO) donor for heart failure with positive lusitropic and inotropic as well as vasodilatory effects. Cimlanod delivers HNO via pH-dependent chemical breakdown when exposed to the neutral pH environment of the bloo
T76332	Biotinyl-Glucagon (1-29), human, bovine, porcine
	Biotinyl-Glucagon (1-29), human, bovine, porcine 为带生物素标记的Glucagon衍生物，此肽类激素由胰腺α细胞分泌，功能是提升血液中的葡萄糖与脂肪酸浓度。
T78977	Antitrypanosomal agent 12	Parasite	Microbiology/Virology
	Antitrypanosomal agent 12 是 C20-苯基硫脲化合物，显示出杀锥虫和细胞毒性。该化合物在实现 50% 生长抑制(GI50)时所需浓度为0.22 μM，能在血流形式的锥虫中引起细胞肿胀。
T38503	(2-pyridyldithio)-PEG1-hydrazine (2-pyridyldithio)-PEG1-hydrazine
	(2-Pyridyldithio)-PEG1-hydrazine is a one-unit cleavable polyethylene glycol (PEG) linker specifically designed for the synthesis of antibody-drug conjugates (ADCs). This linker offers the advantage of controlled release of the drug payload from the ADC construct. It is utilized in the conjugation process between the antibody and the cytotoxic drug, enabling the targeted delivery of the drug to cancer cells. The (2-pyridyldithio) group of this linker provides stability during circulation in the ...
T77111	Omodenbamab
	Omodenbamab 是一种抗 SpA(葡萄球菌蛋白 A) 人源化单克隆抗体，KD 值为 0.0467 nM。Omodenbamab 通过靶向细胞壁部分蛋白 A (SpA) 来规避关键的 S. aureus 逃避机制。Omodenbamab 可用于 S. aureus 血流感染的研究。
TP1155	Human growth hormone-releasing factor Growth Hormone Releasing Factor human
	Human growth hormone-releasing factor stimulates GH production and release by binding to the GHRH Receptor (GHRHR) on cells in the anterior pituitary.Growth hormone-releasing hormone is a hormone produced in the hypothalamus. The main role of growth hormo
T73676	MIF-1 TFA
	MIF-1 TFA（Melanostatin）是一种内源性脑肽，具有有效调节多巴胺受体变构的作用，并抑制黑色素生成。此外，它通过阻断阿片受体的激活，调控吗啡的镇痛效果及应激诱导的镇痛（SIA）。MIF-1 TFA 能直接穿过血脑屏障（BBB）进入中枢神经系统。
T64553	GLP-1(7-37) TFA salt
	The truncated glucagon-like peptides GLP-1(7-37) is naturally occurring peptide product of the preproglucagon gene that are synthesized primarily in the intestine and acts as incretin that are released from the intestine into the bloodstream in response to food and stimulate insulin secretion. GLP-1(7-37) produced a dose-related enhancement of the glucose-stimulated increase in plasma insulin concentration and an increased rate of glucose infusion in Sprague-Dawley Rats at a dosing rang of 0.5, ...

化合物

Cat.No: T6532

Target: Influenza Virus, Parasite, Aurora Kinase, Autophagy

Probucol disuccinate

Cat.No: T4179

Target: LDL

Cat.No: T4582

Synonym: NSC 4038,占吨氢醇

Target: Others

Histrelin acetate

Cat.No: TP2107L

Synonym: Histrelin acetate(76712-82-8 free base),醋酸组氨瑞林

Target: GNRH Receptor

Cat.No: T70673

Cat.No: T25490

Synonym: Tyr-pro-trp-thr

Cat.No: T38967

Cat.No: T31215

Synonym: DB766

PEX5-PEX14 PPI-IN-1

Cat.No: T79457

Cat.No: T14967

Synonym: BMS-986231,CXL-1427

Target: Others

Biotinyl-Glucagon (1-29), human, bovine, porcine

Cat.No: T76332

Antitrypanosomal agent 12

Cat.No: T78977

Target: Parasite

(2-pyridyldithio)-PEG1-hydrazine

Cat.No: T38503

Synonym: (2-pyridyldithio)-PEG1-hydrazine

Cat.No: T77111

Human growth hormone-releasing factor

Cat.No: TP1155

Synonym: Growth Hormone Releasing Factor human

Cat.No: T73676

GLP-1(7-37) TFA salt

Cat.No: T64553

Cat. No.	Product Name	Target	Signaling Pathways
T0254	Probucol DH-581,普罗布考	Virus Protease; ABC; Lipid	Membrane transporter/Ion channel; Metabolism; Microbiology/Virology
	Probucol (DH-581) 是一种抗高脂血症药物，可通过增加 LDL 分解代谢率来降低血液中的胆固醇水平。
TN1051	1-Caffeoylquinic acid 金银花,1-咖啡酰奎宁酸	NF-κB	NF-κB
	1-Caffeoylquinic acid 是一种有效的NF-κB 抑制剂，对 p105 的 RH 结构域显示高结合亲和力，Ki= 0.002 μM，结合能为 1.50 Kcal/mol。它抑制PD-1/PD-L1相互作用。它具有抗氧化应激能力。
T4776	Glycerol Glycerin,甘油	Endogenous Metabolite	Metabolism
	Glycerol 是甘油三酯（即脂肪和油）和磷脂的重要成分。它在食品工业中被广泛用作甜味剂和保湿剂以及药物制剂。
TN2515	1,7-Bis(4-hydroxyphenyl)hepta-4,6-dien-3-one	Antifection	Microbiology/Virology
	(4Z,6E)-5-hydroxy-1,7-bis(4-hydroxyphenyl)hepta-4,6-dien-3-one shows growth inhibitory activity in vitro versus bloodstream forms of African trypanosomes, with the IC(50) value in the range of 1-3 microg/mL.
T83903	Polymyxin B2 sulfate
	Polymyxin B2是一种抗生素，并且是从B. polymyxa分离出的阳离子脂肽抗生素polymyxin B的主要成分。该化合物对P. aeruginosa、A. baumannii、K. pneumoniae和E. cloacae菌株具有活性（MICs分别为1-2、0.5-1、0.25-0.5和0.25-1 µg/ml）。在体内实验中，以4 mg/kg剂量的Polymyxin B2能显著降低P. aeruginosa血液感染小鼠模型中的血液集落形成单位(CFUs)数量。

天然产物

Cat.No: T0254

Synonym: DH-581,普罗布考

Target: Virus Protease, ABC, Lipid

1-Caffeoylquinic acid

Cat.No: TN1051

Synonym: 金银花,1-咖啡酰奎宁酸

Target: NF-κB

Cat.No: T4776

Synonym: Glycerin,甘油

Target: Endogenous Metabolite

1,7-Bis(4-hydroxyphenyl)hepta-4,6-dien-3-one

Cat.No: TN2515

Target: Antifection

Polymyxin B2 sulfate

Cat.No: T83903

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